(3-Bromobicyclo[1.1.1]pentan-1-yl)methanol

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Reagent Code: #152417
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CAS Number 137741-16-3

science Other reagents with same CAS 137741-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.04 g/mol
Formula C₆H₉BrO
badge Registry Numbers
MDL Number MFCD31705883
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as a building block in medicinal chemistry, this compound enables the synthesis of highly strained, three-dimensional structures that improve drug potency and metabolic stability. Its unique bridged architecture is valuable in the design of bioisosteres, particularly as a replacement for phenyl or tert-butyl groups, enhancing pharmacokinetic properties in drug candidates. It is especially useful in the development of CNS-targeted therapeutics due to its ability to increase saturation and reduce planarity, which can improve blood-brain barrier penetration. Additionally, the hydroxyl group allows for further functionalization, facilitating conjugation or linker attachment in prodrug strategies and targeted therapies.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿13,550.00
inventory 100mg
10-20 days ฿21,330.00
inventory 250mg
10-20 days ฿43,010.00

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(3-Bromobicyclo[1.1.1]pentan-1-yl)methanol
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Used primarily as a building block in medicinal chemistry, this compound enables the synthesis of highly strained, three-dimensional structures that improve drug potency and metabolic stability. Its unique bridged architecture is valuable in the design of bioisosteres, particularly as a replacement for phenyl or tert-butyl groups, enhancing pharmacokinetic properties in drug candidates. It is especially useful in the development of CNS-targeted therapeutics due to its ability to increase saturation and r

Used primarily as a building block in medicinal chemistry, this compound enables the synthesis of highly strained, three-dimensional structures that improve drug potency and metabolic stability. Its unique bridged architecture is valuable in the design of bioisosteres, particularly as a replacement for phenyl or tert-butyl groups, enhancing pharmacokinetic properties in drug candidates. It is especially useful in the development of CNS-targeted therapeutics due to its ability to increase saturation and reduce planarity, which can improve blood-brain barrier penetration. Additionally, the hydroxyl group allows for further functionalization, facilitating conjugation or linker attachment in prodrug strategies and targeted therapies.

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